The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
124576773 12457677 3 F 20160429 20160713 20160610 20160810 PER US-009507513-1605USA010901 MERCK 64.12 YR F Y 90.70000 KG 20160810 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
124576773 12457677 1 PS JANUMET XR METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 50/1000 TABLET DAILY 15 DF 22044 1 DF PROLONGED-RELEASE TABLET QD
124576773 12457677 2 SS JANUMET XR METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral UNK 15 DF 22044 PROLONGED-RELEASE TABLET
124576773 12457677 3 SS JANUMET XR METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 100/1000 MG TABLET DAILY 3 DF Y M004523 22044 1 DF PROLONGED-RELEASE TABLET QD
124576773 12457677 4 C NORVASC AMLODIPINE BESYLATE 1 U 0
124576773 12457677 5 C LOSARTAN POTASSIUM TABLETS LOSARTAN POTASSIUM 1 U 0 POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124576773 12457677 1 Diabetes mellitus
124576773 12457677 3 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124576773 12457677 Abdominal discomfort
124576773 12457677 Abdominal pain
124576773 12457677 Anorectal discomfort
124576773 12457677 Diarrhoea
124576773 12457677 Product use issue
124576773 12457677 Swelling

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
124576773 12457677 1 20160429 20160513 0
124576773 12457677 2 201606 0
124576773 12457677 3 20160512 20160615 0